US4521567A - Method for making impact resistant molding compositions - Google Patents

Method for making impact resistant molding compositions Download PDF

Info

Publication number
US4521567A
US4521567A US06/637,863 US63786384A US4521567A US 4521567 A US4521567 A US 4521567A US 63786384 A US63786384 A US 63786384A US 4521567 A US4521567 A US 4521567A
Authority
US
United States
Prior art keywords
monomers
phase
stage
polymerization
polymer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US06/637,863
Other languages
English (en)
Inventor
Peter J. Arndt
Walter Ludwig
Manfred Munzer
Werner Siol
Franz Wenzel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Roehm GmbH Darmstadt
Original Assignee
Roehm GmbH Darmstadt
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Roehm GmbH Darmstadt filed Critical Roehm GmbH Darmstadt
Assigned to ROHM GMBH reassignment ROHM GMBH ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: ARNDT, PETER J., LUDWIG, WALTER, MUNZER, MANFRED, SIOL, WERNER, WENZEL, FRANZ
Application granted granted Critical
Publication of US4521567A publication Critical patent/US4521567A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
    • C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S525/902—Core-shell

Definitions

  • the present invention relates to a method for making impact resistant molding compositions, and particularly of crystal clear molding compositions, by means of a two stage polymerization process.
  • Polymers modified to improve their impact strength generally are multiphase materials comprising at least a hard phase and a rubbery phase.
  • Such polymers are produced commercially mainly by emulsion polymerization since discrete rubbery phase particles coated with a hard phase can readily be produced by this method.
  • the advantages inherent in this method are partly offset by the considerable difficulties and costs which isolation of the solid polymer entails.
  • the polymerization auxiliaries used cannot always be removed to the desired extent. It has therefore been sought to produce impact resistant molding compositions by methods other than emulsion polymerization, for example by bulk or bead (suspension) polymerization.
  • insoluble monomers are dispersed by mechanical action (agitation) in a nonsolvent (the continuous phase) and polymerized, generally by the use of initiators insoluble in the continuous phase.
  • the polymer formed is predominantly soluble in the monomer.
  • the monomer forms spherical droplets.
  • dispersing agents protective colloids
  • the continuous phase usually is water.
  • a method for making impact resistant bead polymers is described in U.S. Pat. No. 3,458,603. In that multiple stage process, the bead polymerization of methyl methacrylate and/or styrene is carried out in a first stage in the presence of dispersing agents and with the formation of a first aqueous dispersion. Bead polymerization is then continued in this first dispersion in a second stage with a monomer mixture of C 1 to C 8 alkyl acrylates together with from 0.01 to 10 weight percent of a crosslinking agent, with formation of a second aqueous dispersion.
  • Bead polymerization is then completed in this second dispersion in a third stage after the addition of methyl methacrylate and/or styrene.
  • the monomers may contain up to 50 weight percent of another copolymerizable monomer.
  • Each process stage should be carried to complete polymerization of the monomers present.
  • the molecular weight of the polymers may be controlled conventionally.
  • U.S. Pat. No. 3,943,190 also proposes impact resistant bead polymers which are produced by a two stage process.
  • the hard phase consisting of methyl methacrylate with from 0 to 40 weight percent of a C 1 to C 8 acrylic ester and from 0 to 10 weight percent of a vinyl monomer copolymerizable with said ester, is polymerized in the first stage and the soft phase, formed from 89 to 99.9 weight percent of alkyl acrylate, from 0.1 to 3 weight percent of crosslinking agent, and optional alkyl methacrylate, is polymerized in the second stage.
  • the weight ratio of the monomers polymerized in the first stage to the monomers polymerized in the second stage must be 100:20-70.
  • transparent, weather resistant, and impact resistant polymers are obtained by multiple stage suspension polymerization.
  • the hard phase consisting of 50 to 100 weight percent of methyl methacrylate, is polymerized first.
  • a mixture of an acrylic ester, from 0 to 10 weight percent of alkyl methacrylate, from 0.1 to 3 weight percent of crosslinking agent, and from 1 to 30 weight percent of a comonomer for matching the refractive index to that of the hard phase is added and the particles of the hard phase are impregnated therewith.
  • the suspension polymerization is then carried to completion.
  • Japanese patent publication No. 78-138496 (Chem. Abstr. 90, 122484q) also relates to transparent, impact resistant polymethyl methacrylate resins.
  • First the hard phase is produced by polymerization in water at 80° C. using a redox catalyst system consisting of a chain transfer agent, a persulfate, and a reducing sulfoxy compound in the absence of an emulsifier.
  • a monomer mixture formed of 50 to 90 weight percent of alkyl acrylate, 3 to 40 weight percent of methyl methacrylate, 0 to 40 weight percent of further unsaturated comonomers, 0.1 to 5 weight percent of allyl or methallyl and crotyl esters of unsaturated carboxylic and dicarboxylic acids, and 0 to 5 weight percent polyfunctional crosslinking agents is then added to the emulsion and the mixture so obtained is polymerized in the absence of an emulsifier.
  • Japanese patent publication No. 78-36589 discloses impact resistant materials obtained by the polymerization of methyl methacrylate, optionally together with other monomers, in an aqueous suspension in the presence of a chain transfer agent, followed by the addition of 5 to 40 percent, by weight of the resin, of monomers which form a latexlike polymer, 0.01 to 2 mole percent of polyfunctional monomers, and 0.05 to 10 mole percent of an oil soluble peroxide and polymerization of this mixture.
  • the method of the present invention is a bulk (mass) polymerization or a bead (suspension) polymerization in an aqueous medium which comprises, in a first stage, the polymerization of a hard phase (A) having a glass transition temperature above 25° C.
  • Polymerization of the hard phase (A) in the first stage is carried out in the presence of (a) an oil soluble free radical initiator and of (b) an organosulfur chain transfer agent with at least two thiol groups in the molecule.
  • Polymerization of the rubbery phase (B) is carried out in the presence of the hard phase (A) by swelling the previously formed hard phase (A) with the monomers. Polymerization of the monomers of the rubbery phase thus takes place substantially within the preformed hard phase. Polymerization is advantageously carried out using the residual initiator still present in the hard phase.
  • T g glass transition temperatures
  • the glass transition temperature of the hard phase (A) polymerized in the first stage usually is above 25° C., and preferably is 60° C. or higher.
  • alkyl esters of acrylic acid are methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, butyl acrylate, and particularly n-butyl and isobutyl acrylate, n-hexyl acrylate and 2-ethylhexyl acrylate, as well as neopentyl acrylate.
  • alkyl esters of methacrylic acid with C 2 to C 8 alcohols examples include ethyl methacrylate, n-propyl methacrylate, butyl methacrylate, and particularly n-butyl methacrylate.
  • esters may also be used in the form of mixtures.
  • Examples of other vinyl monomers which are copolymerizable in amounts from 0 to 10 weight percent with said esters are aromatic vinyl compounds, for example styrene and its derivatives such as alpha-methylstyrene and para-methylstyrene, as well as vinyl esters of aromatic or aliphatic carboxylic acids such as vinyl acetate and vinyl benzoate, as well as acrylonitrile and methacrylonitrile.
  • aromatic vinyl compounds for example styrene and its derivatives such as alpha-methylstyrene and para-methylstyrene
  • vinyl esters of aromatic or aliphatic carboxylic acids such as vinyl acetate and vinyl benzoate, as well as acrylonitrile and methacrylonitrile.
  • the monomers of the rubbery phase (B) are defined as those which, in the form of homopolymers or copolymers (independently of the hard phase), have a glass transition temperature below 25° C., and preferably below 10° C.
  • Suitable esters of methacrylic acid are the esters of C 2 to C 8 alcohols named above and suitable esters of methacrylic acid are those of C 1 to C 8 alcohols.
  • Organosulfur chain transfer agents having at least two thiol groups in the molecule generally have at least 2, and preferably at least 6, but usually not more than 40, carbon atoms in the molecule.
  • the presence of one or, preferably, more alpha-mercapto carboxylic ester groups in the molecule, preferably derived from polyols such as glycol, propanediol, glycerol, pentaerythritol, and the like is of advantage.
  • pentaerythritol tetrathioglycolate pentaerythritol tetramercaptopropionate
  • glycol dimercaptoacetate glycol dimercaptopropionate
  • glycerine trithioglycolate trimethylolpropane trithioglycolate
  • trimethylolethane triethioglycolate is especially preferred.
  • Suitable alkanedithiols which can be used are, for example, 1,2-ethanedithiol, 1,3-propanedithiol, 1,4-butanedithiol, 1,5-pentanedithiol, 1,6-hexanedithiol, 1,8-octanedithiol, 1,9-nonanedithiol, and 1,10-decanediethiol.
  • bis-2-mercaptoethyl sulfide should be mentioned (cf. N. Kharasch, Organic Sulfur Compounds, Vol. 1, pp. 199-209, Pergamon Press, New York, 1961).
  • Organosulfur chain transfer agents having at least two thiol groups in the molecule may be represented in part by the formula
  • A is a hydrocarbon chain having from 3 to 16 carbon atoms in which one or more carbon atoms can be replaced by --S--, and more particularly such a hydrocarbon chain having from 4 to 8 carbon atoms, or A is ##STR1## wherein n is 0 or an integer from 1 to 8, and more particularly 0 or 1 to 5, and Y is a hydrocarbon chain having from 2 to 16 carbon atoms which may be substituted with ##STR2## wherein n' has the same meaning as n, and m is 0 or an integer from 1 to 8.
  • the content of organosulfur molecular weight regulators in the polymerization of the hard phase (A) in the first stage generally ranges from 0.05 to 5 percent, and preferably from 0.1 to 2 percent, by weight of the hard phase (A).
  • Suitable oil soluble (and water insoluble) free radical initiators (a) are, for example, peroxidic and azo compounds of that type (cf. U.S. Pat. No. 2,471,959). These include organic peroxides such as dibenzoyl peroxide or dilauroyl peroxide and peresters such as tert-butyl-peroxy-2-ethylhexanoate, as well as azo compounds such as azoisobutyronitrile and other known initiators of this type. Free radical forming initiators having higher decomposition temperatures may additionally be used, for example if the temperature is raised toward the end of the reaction to obtain as nearly complete polymerization as possible.
  • the amount of the oil soluble free radical initiators generally ranges from 0.01 to 5 percent, and preferably from 0.2 to 3 percent, and still more preferably is 1.5 ⁇ 1 percent, by weight of the monomers of the hard phase (A).
  • the graft crosslinkers which are used in stage (B) in accordance with the invention are either monomers with at least two different polymerizable groups having different reactivities in the molecule, or monomers having at least three similar polymerizable groups in the molecule, but which groups similarly have different reactivities. In the latter case, the different reactivities of the polymerizable groups, which are otherwise the same in structure, is probably attributable to steric hindrance of those polymerizable groups in each molecule which are unpolymerized as the polymerization proceeds.
  • Both types of graft crosslinker that is monomers with at least two polymerizable groups but different reactivities in the molecule and monomers with at least three similar polymerizable groups in the molecule, will improve the clarity of the impact resistant molding compositions. It may be assumed that these graft crosslinkers aid in preventing the divergent polymerization of the monomers having different refractive indices. Moreover, both types of graft crosslinker improve thermoplastic processability (e.g the extrudability) of the material in comparison with other crosslinking agents such as butanediol dimethylacrylate.
  • the graft crosslinkers having at least two polymerizable entities having different reactivities may be represented by the general formula ##STR3## wherein Q is --O-- or --NR 5 , where R 5 is hydrogen or C 1 -C 6 alkyl,
  • R 1 , R 1 ', R 1 ", R 2 and R 2 ' are, independently of each other, hydrogen or methyl
  • Examples are the allyl, methallyl, and crotyl esters of ⁇ , ⁇ -unsaturated carboxylic acids, such as allyl metnacrylate and allyl acrylate, and the corresponding methallyl, crotyl, and vinyl esters.
  • An example of a graft crosslinker having three similar polymerizable units in the molecule is trimethylolpropane triacrylate.
  • Other examples of graft crosslinkers are trimethylolpropane trimethacrylate, glycerine trimethacrylate and triacrylate, vinyl methacrylate and vinyl acrylate, vinyloxyethylmethacrylate, N-allylmethacrylamide, and N-allylacrylamide.
  • the refractive indices of the hard phase (A) and of the rubbery phase (B) may match or differ depending on the monomers selected.
  • the polymers of the hard phase (A) and of the rubbery phase (B) should have at least about the same refractive index.
  • copolymerizable monomers making different contributions to the refractive index may be conventionally incorporated in the polymers, for example monomers with fairly high optical density, suitably aromatic monomers, and particularly monomers having a phenyl group therein such as styrene and its derivatives and homologs like alpha-methylstyrene and para-methylstyrene. Their amount will generally range from 10 to 30 percent, by weight of the monomers of the rubbery phase.
  • the good mechanical properties of the impact resistant molding compositions of the invention depend primarily on the use in the hard phase (A) of an organosulfur molecular weight regulator having at least two thiol groups in the molecule.
  • the nature of the crosslinker used in the rubbery phase (B), on the other hand, has a very marked effect on the optical properties and processing characteristics of the material. For example, when a graft crosslinker having at least two polymerizable entities of different reactivity in the molecule, or when crosslinkers having at least three similar polymerizable groups in the molecule, are used, the products will be decidedly clearer than are products obtained by the use of other crosslinking agents. Also, such molding compositions will be much more readily extrudable than molding compositions produced by the use of other crosslinking agents.
  • the method for the invention may be carried out along the lines of the known bead (suspension) or bulk polymerization processes, bead polymerization being the preferred mode of operation.
  • bead polymerization the ratio of the aqueous phase to the monomer phase usually ranges from 1.5:1 to 4:1.
  • the commonly used dispersing agents should be employed, generally in amounts not exceeding a few weight percent based on the aqueous phase.
  • Suitable dispersants include water insoluble salts of inorganic acids, such as barium sulfate or barium carbonate, water insoluble oxides such as aluminum hydroxide, or high molecular weight natural substances or synthetic polymers.
  • the group of high molecular weight dispersants includes water soluble colloids such as polyvinyl alcohol, partially saponified polyvinyl acetate, methyl cellulose, starch, gelatin, pectin, the alkali metal salts of polyacrylic acid, or the alkali metal salts of styrene or vinyl acetate/maleic anhydride copolymers, etc.
  • a guide value for the amount of dispersant to be used is 1 weight percent, for example, based on the monomers used.
  • the bead polymerization will be carried out at a temperature ranging from 50° to 95° C.
  • the polymerization time is dependent in large measure on the other process parameters but usually ranges from 2 to 10 hours.
  • initiator will primarily be used in the final polymerization.
  • the dispersing agents used in bead polymerization permit the hard phase (A) to be readily swollen with the monomers of the rubbery phase (B), there appear to be no limitations.
  • Particularly preferred are the so called organic dispersants, for example partially saponified polyvinyl acetate, alkali metal salts of sytrene or vinyl acetate/maleic acid copolymers, and other polymers having hydrophobic and hydrophilic groups in the same molecule.
  • a salt for example common salt, may be added to the aqueous phase.
  • low molecular weight emulsifiers such as the sodium salts of alkanesulfonic acids may also concurrently be used.
  • the size of the bead polymers may vary from a few microns to several millimeters. As a rule, however, the bead size will be held within a range of about 20 microns to about 2 mm. This assures (1) a large surface area that will permit the hard phase (A) polymerized first to be rapidly swollen with the monomers of the rubbery phase (B) and (2) a bead size that will permit the beads to be readily separated from the aqueous phase.
  • the bead polymerization of the hard phase (A) and that of the monomers (B) will usually be performed sequentially in the same polymerization vessel. However, the two polymerization stages can also be carried out sequentially in two different polymerization vessels.
  • the monomers of the hard phase (A) will generally have been polymerized to the extent of at least 80 weight percent by the time the monomers of the rubbery phase (B) are added. It is highly advantageous to add the monomers of the rubbery phase only after the gel-effect has set in in phase (A). The addition of the monomers of the rubbery phase (B) thus takes place at a time when the maximum rate of polymerization of the hard phase has passed. (With regard to the gel-effect, see H. Rauch-Puntigam and Th. Volker in "Acryl- und Methacrylitatien", Springer-Verlag, 1967.)
  • polymerization may also be carried out by first producing the hard phase by bulk (mass) polymerization and then, after the hard phase (A) has been comminuted to increase the surface area (unless it was actually produced in a high surface form, such as a polymer string), swelling it with the monomers of the rubbery phase (B) and polymerizing the latter monomers in the presence of the hard phase (A).
  • the process may also be carried out by first polymerizing the hard phase (A) by the bead polymerization technique and then performing the polymerization of the monomers of the rubbery phase (B) within the hard phase (A) as a bulk polymerization.
  • two stage bead polymerization is the preferred mode of operation.
  • any other process in which the polymer is obtained directly in the form of readily isolated particles having a weight of at least 10 -9 g/particle and wherein the preformed hard phase (A) can readily be swollen with the monomers of the rubbery phase (B) should be suitable.
  • Emulsion polymerization in which the polymer particles usually have a weight of less than 10 -12 g/particle, thus must be ruled out since, following the actual polymerization process, that method requires the performance of costly operations for isolation of the solid polymer, for example chemical precipitation, spray drying, etc.
  • the weight ratio of the monomers of the hard phase (A) to the monomers of the rubbery phase (B) should range from 1:0.15 to 1:3 and preferably from 1:0.25 to 1:1.5.
  • thermoplastically processable molding composition used in such mixing is advantageously composed of polymethyl methacrylate. Mixing is advantageously done under high shear stresses, for example by means of a kneading extruder or of a co-kneader.
  • Additives such as solvents, plasticizers (e.g. dioctyl phthalate), or lubricants (e.g. cetyl alcohol or paraffin) may be used both in the production of the two stage polymer according to the invention and in mixing it with other molding compositions.
  • lubricants e.g. cetyl alcohol or paraffin
  • Other low molecular weight substances such as anti-aging agents, dyes, etc. may also be added.
  • the organosulfur chain transfer agent (B) of the invention having at least two thiol groups in the molecule is not used, the presence of this component is of great importance to the mechanical properties of the impact resistant molding compositions.
  • Good optical properties of the impact resistant molded articles and good processability of the molding composition further require the use of a graft crosslinker in the monomer mixture (B).
  • an 0.4% dispersant solution for example aluminum hydroxide prepared in situ from aluminum sulfate and soda, was used.
  • polyvinyl alcohol was used in the presence of 0.05 weight percent of the sodium salt of a C 14 to C 16 alkanesulfonic acid.
  • alkanethiol such as 1,6-hexanedithiol can be employed as a chain transfer agent in the method of this Example, instead of pentaerythritol tetrathioglycolate.
  • Example 2 The same bead polymerization recipe is used as in Example 1. However, a trifunctional crosslinker is used in the monomer mixture (B).
  • Example 2 The same procedure is followed as in Example 1 except that a different graft crosslinker is used in the monomer mixture (B).
  • Example 3 The same procedure is followed as in Example 3 except that a MW having only one thiol group in the molecule is used in place of the tetrafunctional organosulfur chain transfer agent.
  • Example 2 The same procedure is followed as in Example 1 except that a regulator having only one thiol group in the molecule is used in place of tetrafunctional chain transfer agent.
  • a polymer is obtained which does yield clear molded articles. However, the mechanical properties of such articles are quite inferior compared with articles made with the polymer of Example 1. In contrast to the molding composition of Example 1, the material of Example 5 is not extrudable.
  • Example 2 The same procedure is followed as in Example 1 except that no graft crosslinker is used in monomer mixture (B).
  • Example 2 The same procedure is followed as in Example 1 except that no polyfunctional organosulfur chain transfer agent is used in phase (A) and no graft crosslinker is used in phase (B).
  • a material is obtained which when used in molding compositions for injection molding results in opaque articles with poor mechanical properties.
  • the composition is not extrudable. See also Table 1.
  • the bead polymer of Example 1 is granulated in a kneading extruder.
  • a molding composition is so obtained which can be injection molded or extruded to give crystal clear impact resistant articles.
  • Example 2 The same procedure is followed as in Example 1, but a different weight ratio of hard phase (A) to rubbery phase (B) is selected.
  • the beads were worked up as described in Example 1. Mixing them with a thermoplastically processable polymethyl methacrylate in a ratio of 1:1 results in a molding composition which can be injection molded or extruded to give clear, impact resistant articles.
  • This example relates to a two stage process for the production of an impact resistant molding composition wherein the first stage is carried out as a bead polymerization and the second stage as a bulk polymerization.
  • Polymerization of the hard phase (A) is performed as described in Example 1. However, the recipe is three times as large.
  • Polymerization is carried out with vigorous agitation for 120 minutes at 70° C. This is followed by cooling, washing out the dispersant, and drying at room temperature.
  • the batch is gradually heated to 45° C., which produces a highly viscous solution.
  • the latter is used to fill five bags of equal size. These bags are then polymerized, initially for 30 minutes at 55° C., then for 3 hours at 60° C., then for 2 hours at 65° C., then for 3 hours at 70° C., and finally for 5 hours at 90° C.
  • the samples are then cooled and comminuted.
  • the comminuted polymer is then mixed in a ratio of 1:1 with a thermoplastically processable polymethyl methacrylate and extruded.
  • the extrudate is used to injection mold test pieces.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Graft Or Block Polymers (AREA)
  • Polymerisation Methods In General (AREA)
US06/637,863 1983-08-18 1984-08-06 Method for making impact resistant molding compositions Expired - Lifetime US4521567A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3329765A DE3329765C2 (de) 1983-08-18 1983-08-18 Verfahren zur Herstellung schlagzäher Formmassen auf Acrylatbasis durch zweistufige Polymerisation
DE3329765 1983-08-18

Publications (1)

Publication Number Publication Date
US4521567A true US4521567A (en) 1985-06-04

Family

ID=6206806

Family Applications (1)

Application Number Title Priority Date Filing Date
US06/637,863 Expired - Lifetime US4521567A (en) 1983-08-18 1984-08-06 Method for making impact resistant molding compositions

Country Status (6)

Country Link
US (1) US4521567A (enrdf_load_stackoverflow)
JP (1) JPS6060119A (enrdf_load_stackoverflow)
DE (1) DE3329765C2 (enrdf_load_stackoverflow)
FR (1) FR2550793B1 (enrdf_load_stackoverflow)
GB (1) GB2148908B (enrdf_load_stackoverflow)
IT (1) IT1179059B (enrdf_load_stackoverflow)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4737533A (en) * 1986-04-15 1988-04-12 Rhone-Poulenc Chimie Dry material which can be hydrated into an aqueous gel, containing dispersed polymer particles, process for the preparation thereof and use thereof in biological applications
US5006593A (en) * 1988-06-16 1991-04-09 E. I. Du Pont De Nemours And Company Catenated polymer systems
US5102939A (en) * 1985-11-30 1992-04-07 Bayer Aktiengesellschaft Mixtures suitable as stabilizers for polymers
US5155172A (en) * 1989-01-30 1992-10-13 Rohm Gmbh Chemische Fabrik Elastomeric acrylic resins
US5198500A (en) * 1990-01-16 1993-03-30 Nippon Paint Co., Ltd. Process for preparing crosslinked resin particles
US20020173589A1 (en) * 2001-05-15 2002-11-21 Mitsubishi Gas Chemical Company, Inc. Acrylic syrup and method of producing same
US20060058458A1 (en) * 2002-12-19 2006-03-16 Roehm Gmbh & Co. Kg Coating agents for producing rigid coatings resistant to scratching and soiling and rigid moulded bodies resistant to scratching and soiling and method for the production thereof
US7784161B2 (en) 2006-03-27 2010-08-31 Rotox Gmbh Device for machining the corner area of a frame welded together out of profiled pieces
WO2011003219A1 (en) * 2009-07-07 2011-01-13 Evonik Röhm Gmbh Plasties moulding compositions, mouldings and production processes
US20110210454A1 (en) * 2008-11-21 2011-09-01 Allison Yue Xiao Phase Separated Curable Compositions
DE102010028186A1 (de) 2010-04-26 2011-10-27 Evonik Röhm Gmbh Fluoreszenzkonversionssolarzelle Lacke

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61272206A (ja) * 1985-05-28 1986-12-02 Asahi Chem Ind Co Ltd 耐熱分解性に優れたメタクリル樹脂の製造法
JPS61272215A (ja) * 1985-05-29 1986-12-02 Asahi Chem Ind Co Ltd 耐熱耐溶剤性アクリル共重合体の製造方法
DE4141319A1 (de) * 1991-12-14 1993-10-14 Roehm Gmbh Hochschlagzähe Polymermischungen
US6410005B1 (en) 2000-06-15 2002-06-25 Pmd Holdings Corp. Branched/block copolymers for treatment of keratinous substrates
DE10101389A1 (de) 2001-01-13 2002-07-18 Roehm Gmbh Unsymmetrische (Meth)acrylatvernetzer
DE102005003303A1 (de) * 2005-01-24 2006-07-27 Röhm GmbH & Co. KG Thio(meth)acrylate, Mischungen zur Herstellung transparenter Kunststoffe, transparente Kunststoffe sowie Verfahren zu deren Herstellung und Verwendung
JP6222869B1 (ja) * 2016-07-29 2017-11-01 サイデン化学株式会社 無溶剤液状アクリル樹脂組成物及び無溶剤液状アクリル樹脂組成物の製造方法
EP3369788B1 (en) * 2017-03-03 2019-05-08 Evonik Röhm GmbH Curable thermosetting resin compositions with improved mechanical properties

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3458603A (en) * 1965-12-10 1969-07-29 Ici Ltd Polymeric styrene or alkyl methacrylate copolymers made by 3-stage granular polymerization process
US3711576A (en) * 1967-09-01 1973-01-16 Stauffer Chemical Co Polymercaptan modified vinyl halide polymers and blends thereof with vinyl halide polymer
US3943190A (en) * 1973-08-15 1976-03-09 Asahi Kasei Kogyo Kabushiki Kaisha Process for preparing acrylate polymers

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3364182A (en) * 1965-10-07 1968-01-16 American Cyanamid Co Polymerization of methyl methacrylate in the presence of a polythiol
JPS5910369B2 (ja) * 1976-03-19 1984-03-08 株式会社クラレ メタクリル樹脂組成物の製法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3458603A (en) * 1965-12-10 1969-07-29 Ici Ltd Polymeric styrene or alkyl methacrylate copolymers made by 3-stage granular polymerization process
US3711576A (en) * 1967-09-01 1973-01-16 Stauffer Chemical Co Polymercaptan modified vinyl halide polymers and blends thereof with vinyl halide polymer
US3943190A (en) * 1973-08-15 1976-03-09 Asahi Kasei Kogyo Kabushiki Kaisha Process for preparing acrylate polymers

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Abstract Japanese Pat. Nos. 53138 496, 53036 589, Kuraray. *
Abstract-Japanese Pat. Nos. 53138-496, 53036-589, Kuraray.

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5102939A (en) * 1985-11-30 1992-04-07 Bayer Aktiengesellschaft Mixtures suitable as stabilizers for polymers
US4737533A (en) * 1986-04-15 1988-04-12 Rhone-Poulenc Chimie Dry material which can be hydrated into an aqueous gel, containing dispersed polymer particles, process for the preparation thereof and use thereof in biological applications
US5006593A (en) * 1988-06-16 1991-04-09 E. I. Du Pont De Nemours And Company Catenated polymer systems
US5155172A (en) * 1989-01-30 1992-10-13 Rohm Gmbh Chemische Fabrik Elastomeric acrylic resins
US5280073A (en) * 1989-01-30 1994-01-18 Rohm Gmbh Chemische Fabrik Elastomeric arcylic resins
US5198500A (en) * 1990-01-16 1993-03-30 Nippon Paint Co., Ltd. Process for preparing crosslinked resin particles
US20020173589A1 (en) * 2001-05-15 2002-11-21 Mitsubishi Gas Chemical Company, Inc. Acrylic syrup and method of producing same
EP1258501A3 (en) * 2001-05-15 2003-07-30 Mitsubishi Gas Chemical Company, Inc. Acrylic syrup and method of producing the same
US7056984B2 (en) 2001-05-15 2006-06-06 Mitsubishi Gas Chemical Co., Inc. Acrylic syrup and method of producing same
US20060058458A1 (en) * 2002-12-19 2006-03-16 Roehm Gmbh & Co. Kg Coating agents for producing rigid coatings resistant to scratching and soiling and rigid moulded bodies resistant to scratching and soiling and method for the production thereof
US7784161B2 (en) 2006-03-27 2010-08-31 Rotox Gmbh Device for machining the corner area of a frame welded together out of profiled pieces
US20110210454A1 (en) * 2008-11-21 2011-09-01 Allison Yue Xiao Phase Separated Curable Compositions
US8426986B2 (en) * 2008-11-21 2013-04-23 Henkel Corporation Phase separated curable compositions
WO2011003219A1 (en) * 2009-07-07 2011-01-13 Evonik Röhm Gmbh Plasties moulding compositions, mouldings and production processes
CN102575081A (zh) * 2009-07-07 2012-07-11 赢创罗姆有限公司 塑料模塑组合物、模制品和制备方法
KR20120095339A (ko) * 2009-07-07 2012-08-28 에보니크 룀 게엠베하 플라스틱 성형 조성물, 성형물 및 제조 방법
US8759450B2 (en) 2009-07-07 2014-06-24 Evonik Röhm Gmbh Plastics moulding compositions, and mouldings and production processes
CN102575081B (zh) * 2009-07-07 2014-12-10 赢创罗姆有限公司 塑料模塑组合物、模制品和制备方法
TWI483984B (zh) * 2009-07-07 2015-05-11 Evonik Roehm Gmbh 塑膠模製組成物、模製品及製造方法
KR101627391B1 (ko) 2009-07-07 2016-06-03 에보니크 룀 게엠베하 플라스틱 성형 조성물, 성형물 및 제조 방법
DE102010028186A1 (de) 2010-04-26 2011-10-27 Evonik Röhm Gmbh Fluoreszenzkonversionssolarzelle Lacke

Also Published As

Publication number Publication date
GB8420846D0 (en) 1984-09-19
IT8467830A0 (it) 1984-08-17
IT1179059B (it) 1987-09-16
IT8467830A1 (it) 1986-02-17
FR2550793B1 (fr) 1988-07-29
GB2148908A (en) 1985-06-05
DE3329765C2 (de) 1993-10-14
FR2550793A1 (fr) 1985-02-22
GB2148908B (en) 1987-02-18
JPH0543727B2 (enrdf_load_stackoverflow) 1993-07-02
JPS6060119A (ja) 1985-04-06
DE3329765A1 (de) 1985-02-28

Similar Documents

Publication Publication Date Title
US4521567A (en) Method for making impact resistant molding compositions
US4246382A (en) Solvent resistent acrylic resin and process for producing the same
US4543383A (en) Impact resistant resins and method for making the same
DE2253689B2 (de) Thermoplastische Masse
JPH0629304B2 (ja) 耐衝撃性改良剤
JPH11511492A (ja) 低いヘイズ値を有する熱可塑性の成形用材料
DE2264224B2 (de) Herstellung eines vernetzten Polystyrol-Emulsionspolymerisats und seine Verwendung zum Trüben von Kunststoffen auf Methacrylstbasis
JPH07258340A (ja) 熱可塑性に加工可能なポリメタクリレート成形材料から製造された押出成形したプレート及びシート、射出成形部品、成形体及び工作部品
KR100301977B1 (ko) 개선된내블록킹성을갖는합성수지분말의제조방법
EP0095769B1 (en) Impact-resistant methacrylic resin composition
KR0160333B1 (ko) 투명성 및 가공성이 우수한 사출성형용 아크릴계 충격보강제의 제조방법
JPH0582405B2 (enrdf_load_stackoverflow)
KR100515592B1 (ko) 열가소성 수지 조성물
JP3539973B2 (ja) 乳化グラフトコポリマー
JPS63120716A (ja) 耐衝撃性樹脂の製造方法
JPH0154361B2 (enrdf_load_stackoverflow)
US3673282A (en) Core-shell vinyl halide polymers having a long-chain vinyl ether containing shell
JPS5942024B2 (ja) 熱可塑性樹脂組成物
JPH09194671A (ja) 硬質熱可塑性メタクリル樹脂組成物から得られる、亀裂発生剤に対して改良された耐性を示す成形品
KR100188529B1 (ko) 저온내충격성 및 광택도가 우수한 열가소성 수지조성물의제조방법
JPH0582406B2 (enrdf_load_stackoverflow)
US4754008A (en) Heat resistant molding compounds
JPS6153350A (ja) 耐溶剤性メタクリル樹脂組成物
JPH0518862B2 (enrdf_load_stackoverflow)
KR20000038610A (ko) 내후성이 우수한 투명 열가소성 수지 조성물 및그의 제조 방법

Legal Events

Date Code Title Description
AS Assignment

Owner name: ROHM GMBH DARMSTADT, GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:ARNDT, PETER J.;LUDWIG, WALTER;MUNZER, MANFRED;AND OTHERS;REEL/FRAME:004339/0373

Effective date: 19840727

Owner name: ROHM GMBH,GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:ARNDT, PETER J.;LUDWIG, WALTER;MUNZER, MANFRED;AND OTHERS;REEL/FRAME:004339/0373

Effective date: 19840727

STCF Information on status: patent grant

Free format text: PATENTED CASE

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 4

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Free format text: PAYER NUMBER DE-ASSIGNED (ORIGINAL EVENT CODE: RMPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 8

FPAY Fee payment

Year of fee payment: 12